Alcohols Production

ABSTRACT

A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application is a nonprovisional PCT application of andclaims benefit of the filing date of copending U.S. provisional patentapplication No. 63/035,073 titled “Alcohols Production” filed Jun. 5,2020 (5 Jun. 2020).

FIELD OF THE INVENTION

The present invention relates to branched alcohols and methods forproducing and manufacturing branched alcohols.

BACKGROUND OF THE INVENTION

This patent application incorporates by reference in its entiretycopending U.S. provisional patent application No. 63/035,073 titled“Alcohols Production” filed Jun. 5, 2020 (5 Jun. 2020).

BACKGROUND OF THE INVENTION

The chemical industry has suffered a long felt need to produce branchedalcohols in a cost-effective manner. There is a ready and large supplyof alpha olefins which are inexpensive. However, there is no known wayto efficiently and cost effectively produce branched alcohols on anindustrial scale using alpha olefins as a feedstock.

SUMMARY OF THE INVENTION

In an embodiment, a process can have the steps of: providing CO and H2;providing a first catalyst which is an organometallic complex of rhodiumand one type of an organophosphorus ligand or an organometallic complexof rhodium and more than one type of an organophosphorus ligand;providing a linear alpha olefin; isomerizing the linear alpha olefin(also herein described as a normal alpha olefin) by the first catalystin the presence of CO and H2 at a first pressure to produce anisomerized olefin; and hydroformylating the isomerized olefin by thefirst catalyst in the presence of CO and H2 at a second pressuredifferent from the first pressure to produce a branched aldehyde. In anembodiment, the branched aldehyde is a 2-alkyl branched aldehyde. In anembodiment, the linear alpha olefin is a C4-C36 linear alpha olefin. Inan embodiment, the branched aldehyde produced from the C4-C36 linearalpha olefin is a C5-C37 branched aldehyde. In an embodiment, the linearalpha olefin can be 1-Butene and the branched aldehyde can be branchedPentanals. In an embodiment, the linear alpha olefin can be 1-Hexene andthe branched aldehyde can be branched Heptanals. In an embodiment, thelinear alpha olefin can be 1-Octene and the branched aldehyde can bebranched Nonanals. In an embodiment, the linear alpha olefin can be1-Decene and the branched aldehyde can be branched Undecanals. In anembodiment, the linear alpha olefin can be 1-Dodecene and the branchedaldehyde can be branched Tridecanals. In an embodiment, the linear alphaolefin can be 1-Tetradecene and the branched aldehyde can be branchedPentadecanals.

In an embodiment, the linear alpha olefin can be 1-Hexadecene and thebranched aldehyde can be branched Heptadecanals. In an embodiment, thelinear alpha olefin can be 1-Octadecene and the branched aldehyde can bebranched Nonadecanals. In an embodiment, the organophosphorous ligandcan be a phosphine. In a nonlimiting example of a phosphine ligand, thephosphine ligand can be triphenylphosphine. In another embodiment, theorganophosphorous ligand can be a phosphite. In a nonlimiting example ofa phosphite ligand, the phosphite ligand can betris(2,4-di-t-butylphenyl)phosphite. In yet another embodiment, amixture of organophosphorous ligands of different types can be used,such as a mixture of a phosphine and a phosphite. In a nonlimitingexample of a mixture of organophosphorous ligands, the organophosphorousligands can be a mixture of triphenylphosphine andtris(2,4-di-t-butylphenyl)phosphite.

In an embodiment, the first catalyst is formed when the molar ratio ofphosphorous to rhodium is in a range of 1:1 to 1000:1. In an embodiment,the first catalyst is formed when the molar ratio of phosphorous torhodium is in a range of 1:1 to 1000:1 in the isomerization step and/orreactor. In an embodiment, the first catalyst is formed when the molarratio of phosphorous to rhodium is in a range of 1:1 to 1000:1 in thehydroformylation step and/or reactor.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention in its several aspects and embodiments solves theproblems discussed above and significantly advances the technology ofbranched compounds and methods for producing and manufacturing branchedcompounds. The present invention can become more fully understood fromthe detailed description and the accompanying drawings, wherein:

FIG. 1 shows an embodiment of a chemical manufacturing process having anisomerization reactor, a hydroformylation reactor, catalyst recovery andan aldehyde hydrogenation reactor;

FIG. 2 shows Sales Specification 1;

FIG. 3 shows Sales Specification 2;

FIG. 4A shows Sales Specification 3, page 1;

FIG. 4B shows Sales Specification 3, page 2;

FIG. 5 shows Sales Specification 4;

FIG. 6A shows Sales Specification 5, page 1;

FIG. 6B shows Sales Specification 5, page 2; and

FIG. 7 shows Sales Specification 6.

Herein, like reference numbers in one figure refer to like referencenumbers in another figure.

DETAILED DESCRIPTION OF THE INVENTION

Described herein is a process for the production of branched C13 and C15aldehydes and alcohols. According to a nonlimiting embodiment of thisprocess, e.g. as shown in FIG. 1 , branched C13 aldehydes (branchedTridecanals) and branched C13 alcohols (branched Tridecanols) can beproduced from a C12 linear alpha olefin (i.e. 1-Dodecene). Examples ofsales specifications for commercially available C12 linear alpha olefinsare shown in FIG. 2 , FIG. 4A/4B, and FIG. 5 . In another embodiment ofthis process, branched C15 aldehydes (branched Pentadecanals) andbranched C15 alcohols (branched Pentadecanols) can be produced from aC14 linear alpha olefin (i.e. 1-Tetradecene). Examples of salesspecifications for commercially available C14 linear alpha olefins areshown in FIG. 3 , FIG. 6A/6B, and FIG. 7 .

A two-step process is disclosed herein which produces highly branchedaldehyde products from linear alpha olefin feedstocks. The two-stepprocess uses a rhodium organophosphorus catalyst for both the firstprocess step and the second step. The first step is an isomerizationreaction step and the second process step is a hydroformylation reactionstep. The highly branched aldehydes can undergo a further hydrogenationstep to produce highly branched alcohols.

Numeric values and ranges herein, unless otherwise stated, also areintended to have associated with them a tolerance and to account forvariances of design and manufacturing. Thus, a number can include values“about” that number. For example, a value X is also intended to beunderstood as “about X”. Likewise, a range of Y-Z, is also intended tobe understood as within a range of from “about Y-about Z”. Unlessotherwise stated, significant digits disclosed for a number are notintended to make the number an exact limiting value. Variance andtolerance are inherent in mechanical design and the numbers disclosedherein are intended to be construed to allow for such factors (innon-limiting e.g., ±10 percent of a given value). Likewise, the claimsare to be broadly construed in their recitations of numbers and ranges.

Every numerical range given throughout this specification will includeevery narrower numerical range that falls within such broader numericalrange, as if such narrower numerical ranges were all expressly writtenherein. As regarding ranges and endpoints, every maximum numericallimitation given throughout this specification includes every lowernumerical limitation, as if such lower numerical limitations wereexpressly written herein. Every minimum numerical limitation giventhroughout this specification will include every higher numericallimitation, as if such higher numerical limitations were expresslywritten herein.

Unless otherwise stated temperatures recited herein are in degreesCelsius (“° C.”).

Unless otherwise stated pressures recited herein are in bar(g), i.e.bars gauge. Herein, 0 bar(g) is atmospheric pressure, e.g. 14.70 psia(aka 0 psig).

Unless otherwise stated percentages of composition recited herein are ona weight basis and disclosed as weight percent (wt. %).

Alternatively, herein, concentration can be expressed in units of partsper million, or ppm.

Herein “branched” is defined as a molecule, compound or chemicalstructure, having one or more alkyl groups attached along a carbonbackbone. “Branched” molecules are isomers of linear (i.e.straight-chain) molecules having the same number of carbon atoms.

Herein, the term “percent branched”, in additional to its ordinary andcustomary meaning, is defined herein to mean the wt. % branchedmolecules in a composition. The term “percent branching” is usesynonymously with “percent branched” and has the same meaning as“percent branched”. As an example, for an aldehyde composition, the“percent branching” of the aldehyde means the wt. % of the aldehydebeing branched, i.e.:

Percent branching %=percent branched %=100*(wt. % branchedaldehyde)+(wt. % branched aldehyde+wt. % linear aldehyde).

As an example, a branched C6 aldehyde composition comprising:

25 wt. % 1-Hexanal (linear molecule) 40 wt. % 2-Methyl-Pentanal(branched molecule) 35 wt. % 2-Ethyl-butanal (branched molecule) wouldhave a Percent Branching = 75%

Unless otherwise stated percent branching recited herein are in weightpercent (wt. %) is calculated based upon reactant and product weights,excluding nonparticipating compounds.

Herein, the term “percent isomerized”, in additional to its ordinary andcustomary meaning, is defined herein to mean the wt. % of olefinmolecules where the olefin has been isomerized from the alpha positionto an internal olefin position. Specifically, the “percent isomerized”means the wt. % of the olefin composition being internal olefins, i.e.:

Percent isomerized %=100*(wt. % internal olefin)+(wt. % alpha olefin+wt.% internal olefin).

As an example, a C12 alpha olefin isomerized to produce a compositioncomprising:

25 wt. % 1-Dodecene (alpha olefin) 40 wt. % 2-Dodecene (internalolefin)) 35 wt. % 3-Dodecene (internal olefin) would have a PercentIsomerized = 75%

Unless otherwise stated the term “internal olefin” recited herein meansan olefin in which a double bond is present in a position other than thealpha position.

Unless otherwise stated percent isomerized recited herein are in weightpercent (wt. %) is calculated based upon reactant and product weights,excluding nonparticipating compounds.

FIG. 1 shows an embodiment of a chemical manufacturing process having anisomerization reactor, a hydroformylation reactor, catalyst recovery andan aldehyde hydrogenation reactor.

FIG. 1 shows an embodiment in which Stream 8 is fed to an aldehydehydrogenation reactor 500 which produces branched alcohols as Stream 12which is a branched alcohols product stream.

FIG. 1 shows an embodiment in which Stream 8 is the feed stream to theAldehyde Hydrogenation Reactor (500) and can have a composition, e.g.:

-   -   1. A C5-C37 aldehyde mixture containing,        -   a. >25 wt. % branched aldehydes,        -   b. <75 wt. % linear aldehydes, and    -   2. Unreacted C4-C36 olefins.

In the embodiment of FIG. 1 , the C5-C37 aldehydes are hydrogenated inthe Aldehyde Hydrogenation Reactor (500) in the presence of hydrogen anda hydrogenation catalyst, e.g. Catalyst A, to produce Stream 12. Stream12 is a branched alcohols product and in an embodiment can have acomposition comprising:

-   -   1. A C5-C37 alcohol mixture containing,        -   a. >30 wt. % branched alcohols,        -   b. <70 wt. % linear alcohols, and    -   2. C4-C36 paraffins (alkanes).

In the embodiment of FIG. 1 , the C5-C37 alcohols are produced from thehydrogenation of the corresponding aldehydes in aldehyde hydrogenationreactor 500 and the C4-C36 paraffins also produced in aldehydehydrogenation reactor 500 resulting from the hydrogenation of theunreacted C4-C36 olefins contained in Stream 8.

Optionally, the C5-C37 alcohols content (purity) can be increased inStream 12, with a related decrease in the C4-C36 paraffin content byusing an optional distillation step after aldehyde hydrogenation reactor500 to remove the low-boiling C4-C36 paraffins and produce a distilled,high purity C5-C37 Branched Alcohols Product which is free of, or nearlyfree of, C4-C36 paraffins.

Stream 1- Alpha Olefin Feed Composition.

Stream 2- Isomerization Reactor Product Composition.

Stream 3- Hydroformylation Product Composition.

Stream 4- Isomerization Reactor Bypass Composition.

Stream 5- Isomerization Reactor Feed Composition.

Stream 6- Hydroformylation Reactor Feed Composition.

Stream 7- Recovered Rhodium Catalyst Stream Composition.

Stream 8- Branched Aldehydes/Unreacted Olefins Composition.

Stream 12- Branched Alcohols Product.

In an embodiment, Stream 12 can be a branched alcohols productcomposition having greater than 40% branching.

In the embodiment of FIG. 1 , the starting Alpha Olefin Feed Compositionis shown as Stream 1. In this embodiment, Stream 1 can be split intoStream 5 (Isomerization Reactor Feed Composition) which is fed toIsomerization Reactor 100 and Stream 4 (Isomerization Reactor BypassComposition) which can be bypassed around Isomerization Reactor 100 andbe provided as a feed to the Hydroformylation reaction. The use of abypass stream, e.g. Stream 4, is optional. It is not necessary to bypassof a portion of the alpha olefin feed around Isomerization Reactor 100;however, using a bypass such as Stream 4 can provide a means to controlthe percentage of alpha olefin isomerization achieved in Stream 6, thefeed stream to Hydroformylation Reactor 200.

In the embodiment of FIG. 1 , the effluent of Isomerization Reactor 100,i.e. Stream 2—Isomerization Reactor Product Composition, is combinedwith Stream 4- Isomerization Reactor Bypass Composition to produceStream 6- Hydroformylation Reactor Feed Composition which is fed toHydroformylation Reactor 200.

In the embodiment of FIG. 1 , Hydroformylation Reactor 200 producesStream 3—Hydroformylation Product Composition.

In the embodiment of FIG. 1 , the Stream 3- Hydroformylation ProductComposition is fed to Catalyst Recovery 300 which produces Stream 7-Recovered Rhodium Catalyst Stream Composition as recycle feed toIsomerization Reactor 100 and Stream 8- Branched Aldehydes/UnreactedOlefins Composition. In FIG. 1 catalyst recovery is shown as occurringin the unit operation shown as Catalyst Recovery 300.

In the embodiment of FIG. 1 , Stream 8- Branched Aldehydes/UnreactedOlefins Composition is fed to Aldehyde Hydrogenation Reactor 500 whichproduces Stream 12, Branched Alcohols Product.

Catalyst Specifications & Composition

The isomerization and hydroformylation reactions disclosed herein can becatalyzed by a rhodium organophosphorus catalyst which can be at leastone of: (1) an organometallic complex of rhodium and one type of anorganophosphorus ligand; (2) or an organometallic complex of rhodium andmore than one type of an organophosphorus ligand.

In an embodiment, the organophosphorous ligand can be a phosphine. In anonlimiting example of a phosphine ligand, the phosphine ligand can betriphenylphosphine. In another embodiment, the organophosphorous ligandcan be a phosphite. In a nonlimiting example of a phosphite ligand, thephosphite ligand can be tris(2,4-di-t-butylphenyl)phosphite. In yetanother embodiment, a mixture of organophosphorous ligands of differenttypes can be used, such as a mixture of a phosphine and a phosphite. Ina nonlimiting example of a mixture of organophosphorous ligands, theorganophosphorous ligands can be a mixture of triphenylphosphine andtris(2,4-di-t-butylphenyl)phosphite. In an embodiment, the reactionsystem can contain an inert high-boiling solvent, for example apolyalphaolefin. In an embodiment, the first catalyst can be formed whenthe molar ratio of phosphorous to rhodium is in a range of 1:1 to1000:1, or 5:1 to 50:1, or 15:1 to 25:1. In an embodiment, the rhodiumconcentration can be in a range of 1 ppm to 1000 ppm, or 10 ppm to 200ppm, or 25 ppm to 75 ppm. In an embodiment, the CO to H2 molar ratio canbe in a range of 10:1 to 1:10, or 2:1 to 1:2, or 1.3:1 to 1:1.3.

Isomerization

In an embodiment, the first process step can be a reaction isomerizing alinear alpha olefin in the presence of Carbon Monoxide (CO) and Hydrogen(H2) at a first pressure. The isomerizing can be catalyzed by therhodium organophosphorus catalyst which can be at least one of: (1) anorganometallic complex of rhodium and one type of an organophosphorusligand; (2) or an organometallic complex of rhodium and more than onetype of an organophosphorus ligand. The isomerization reactions canproduce an isomerized olefin comprising linear internal olefins of thesame or different types.

In an embodiment, the isomerization step can be performed at atemperature in a range of 30° C. to 500° C., or 50° C. to 150° C., or70° C. to 100° C. In an embodiment, the isomerization step can beperformed at a pressure in a range of 0.1 bar(g) to 10 bar(g), or 0.5bar(g) to 5 bar(g), or 1 bar(g) to 2 bar(g).

In an embodiment, the isomerizing step can produce a reaction productcomprising a 20 wt. % or greater isomerized olefin, or a 40 wt. % orgreater isomerized olefin, or a 60 wt. % or greater isomerized olefin,or a 90 wt. % or greater isomerized olefin.

In the embodiment of FIG. 1 , the isomerizing step is shown as occurringin Isomerization Reactor 100.

Hydroformylation

The second process step of this embodiment can be a reactionhydroformylating the isomerized olefin in the presence of CO and H2 at asecond pressure higher than the first pressure to produce a branchedaldehyde. The hydroformylation reaction can be catalyzed by the rhodiumorganophosphorus catalyst which can be at least one of: (1) anorganometallic complex of rhodium and one type of an organophosphorusligand; (2) or an organometallic complex of rhodium and more than onetype of an organophosphorus ligand. In an embodiment, the branchedaldehyde is a 2-alkyl branched aldehyde. In an embodiment, the linearalpha olefin can be 1-Dodecene and the branched aldehyde can be abranched C13 aldehyde. In an embodiment, the linear alpha olefin can be1-Tetradecene and the branched aldehyde can be a branched C15 aldehyde.

In an embodiment, the hydroformylating step can be performed at atemperature in a range of 30° C. to 500° C., or 50° C. to 150° C., or70° C. to 100° C. In an embodiment, the hydroformylating step can beperformed at a pressure in a range of 5 bar(g) to 400 bar(g), or 10bar(g) to 100 bar(g), or 15 bar(g) to 20 bar(g).

In an embodiment, the hydroformylating step can produce a reactionproduct comprising a 25 wt. % or greater branched aldehyde, or a 40 wt.% or greater branched aldehyde, or a 60 wt. % or greater branchedaldehyde, or a 90 wt. % or greater branched aldehyde.

In the embodiment of FIG. 1 , the hydroformylating steps is shown asoccurring in Hydroformylation Reactor 200.

Hydroformylation Product Distillation

In an embodiment, the products of the hydroformylation reaction can bedistilled. In this embodiment, the process can have the step ofseparating the branched aldehyde products resulting fromhydroformylation as an overhead product from the first catalyst streamvia a distillation process. The distillation step can be performed at atemperature in a range of 100° C. to 200° C., or 125° C. to 175° C. Thedistillation step can be performed under vacuum at a pressure of lessthan 500 millibar absolute, or less than 100 millibar absolute, or lessthan 30 millibar absolute.

Hydrogenation

In an embodiment, this process can also have the steps of: hydrogenatingthe branched aldehyde product in the presence of a hydrogenationcatalyst to produce a branched alcohols product composition. In anembodiment, the hydrogenating catalyst can be a base metal catalyst, asupported nickel catalyst, a supported cobalt catalyst, a Raney® (W. R.Grace & Co., 7500 Grace Drive, Columbia, Md. 21044, US, phone1-410-531-4000) nickel catalyst or a precious metal catalyst. In anembodiment, the hydrogenating step can be performed at a temperature ina range of 30° C. to 500° C., or 50° C. to 200° C., or 100° C. to 150°C. In an embodiment, the hydrogenating step can be performed at apressure in a range of 5 bar(g) to 400 bar(g), or 10 bar(g) to 100bar(g), or 30 bar(g) to 50 bar(g).

In the embodiment of FIG. 1 , the step of hydrogenating the branchedaldehyde product in the presence of a hydrogenation catalyst to producea branched alcohols product composition is shown as occurring inAldehyde Hydrogenation Reactor 500.

In an embodiment, the hydrogenating step can produce a reaction productcomprising 25 wt. % or greater branched alcohols, or 40 wt. % or greaterbranched alcohols, or 60 wt. % or greater branched alcohols, or 90 wt. %or greater branched alcohols.

Example 1: Preparation of a Branched C13 Alcohol Product

A C12 linear alpha olefin feedstock (1-Dodecene) was obtained from theChevron Phillips Chemical Company LP, as identified by product nameAlphaPlus® 1-Dodecene (Chevron Phillips Chemical Company LP, P.O. Box4910, The Woodlands, Tex. 77387-4910, US, phone (800) 231-3260). Thehomogeneous rhodium organophosphorus catalyst used in this example isprepared in a high pressure, stainless steel stirred autoclave. To theautoclave was added 0.027 wt. % Rh(CO)2ACAC((Acetylacetonato)dicarbonylrhodium(I)), 1.36 wt. %tris(2,4,-di-t-butylphenyl)phosphite ligand and 98.62 wt. % Synfluid®PAO 4 cSt (Chevron Phillips Chemical Company LP, P.O. Box 4910, TheWoodlands, Tex. 77387-4910, phone (800) 231-3260) inert solvent. Themixture was heated at 80° C. in the presence of a CO/H2 atmosphere and 2bar(g) pressure for four hours to produce the active rhodium catalystsolution (109 ppm rhodium, P:Rh molar ratio=20). The 1-Dodecene linearalpha olefin was added to the rhodium catalyst solution in the autoclaveproducing a starting reaction mixture with a rhodium concentration of 35ppm. The alpha olefin feed was then isomerized at 80° C. in the presenceof a CO/H2 atmosphere and 1 bar(g) pressure for 10 hours. The isomerizedolefin was then hydroformylated at 70° C. in the presence of a CO/H2atmosphere and 20 bar(g) pressure for. 8 hours. The molar ratio of CO toH2 in both the isomerization step and the hydroformylation step wasequal to 1:1.15. The resulting hydroformylation reaction product wasflash distilled at 140-150° C. and 25 millibar to recover the rhodiumcatalyst solution as a bottoms product and recover a branched C13Aldehyde overheads product with a composition comprising:

Weight % 1-Tridecanal 13.9% 2-Methyl-dodecanal 28.3% 2-Ethyl-undecanal15.2% 2-Propyl-decanal 14.5% 2-Butyl-nonanal 13.6% 2-Pentyl-octanal12.6% TOTAL 98.0%

The weight % branching in the branched C13 aldehyde product was 86.2%.

The branched C13 aldehyde product was hydrogenated in a high pressure,Inconel 625 stirred autoclave at 150 C and 20 bar(g) hydrogen pressure.The hydrogenation catalyst used was a Raney® Nickel 3111 (W. R. Grace &Co., 7500 Grace Drive, Columbia, Md. 21044, US, phone 1-410-531-4000)catalyst used at a 0.25 wt. % loading. The aldehyde was hydrogenated for10 hours and the resultant reaction mixture was filtered to produce abranched C13 alcohol product comprising:

Weight % 1-Tridecanol 13.2% 2-Methyl-dodecanol 29.1% 2-Ethyl-undecanol15.5% 2-Propyl-decanol 14.4% 2-Butyl-nonanol 13.2% 2-Pentyl-octanol12.9% TOTAL 98.4%

The weight % branching in the branched C13 alcohol product was 86.6%.

Example 2: Preparation Of A Branched C15 Alcohol Product

The recovered rhodium catalyst stream from Example 1 was charged to ahigh pressure, stainless steel stirred autoclave and a C14 linear alphaolefin feedstock (1-Tetradecene) from the Chevron Phillips ChemicalCompany LP, (AlphaPlus® 1-Tetradecene by Chevron Phillips ChemicalCompany LP, P.O. Box 4910, The Woodlands, Tex. 77387-4910, phone (800)231-3260) was added. The resulting mixture had a rhodium concentrationof approximately 30 ppm. The 1-tetradecene linear alpha olefin was thenisomerized at 80° C. in the presence of a CO/H2 atmosphere and 1 bar(g)pressure for 12 hours. The isomerized olefin was then hydroformylated at70° C. in the presence of a CO/H2 atmosphere and 20 bar(g) pressure for8 hours. The resulting reaction product was flash distilled at 150-160°C. and 25 millibar to recover the rhodium catalyst solution as a bottomsproduct and recover a branched C15 Aldehyde overheads product. Therecovered rhodium catalyst solution was then used again to complete asecond 1-tetradecene batch isomerization (4 hours) and hydroformylation(6 hours). The resulting C15 aldehyde products from the two batches werecombined to give a branched C15 Aldehyde product comprising:

Weight % 1-Pentadecanal 12.1% 2-Methyl-tetradecanal 34.1%2-Ethyl-tridecanal 21.9% 2-Propyl-dodecanal 14.0% 2-Butyl-undecanal 8.6%2-Pentyl-decanal 9.0%* TOTAL 99.6% *This value includes the wt. % of2-hexyl-nonanal.

The weight % branching in the branched C15 aldehyde product was 87.8%.

The branched C15 aldehyde product was hydrogenated in a high pressure,Inconel 625 stirred autoclave at 150 C and 20 bar(g) hydrogen pressure.The hydrogenation catalyst used was a Raney® Nickel 3111 (W. R. Grace &Co., 7500 Grace Drive, Columbia, Md. 21044, US, phone 1-410-531-4000)catalyst used at a 0.25 wt. % loading. The aldehyde was hydrogenated for10 hours and the resultant reaction mixture was filtered to produce abranched C15 alcohol product comprising:

Weight % 1-Pentadecanol 13.7% 2-Methyl-tetradecanol 33.8%2-Ethyl-tridecanol 21.4% 2-Propyl-dodecanol 12.4% 2-Butyl-undecanol 8.0%2-Pentyl-decanol 9.2%* TOTAL 98.4% *This value includes the wt. % of2-hexyl-nonanol.

The weight % branching in the branched C15 aldehyde product was 87.8%.

The weight % branching in the branched C15 alcohols product was 86.1%.

CONCLUSION

This disclosure regards branched compounds and methods for producing andmanufacturing branched compounds in their many aspects, features andelements. Such compounds and manufacturing processes can be dynamic inuse and operation. This disclosure is intended to encompass theequivalents, means, systems and methods of the use of the branchedcompounds and methods for producing and manufacturing branched compoundsand their many aspects consistent with the description and spirit of theapparatus, means, methods, functions and operations disclosed herein.Other embodiments and modifications will be recognized by one ofordinary skill in the art as being enabled by and within the scope ofthis disclosure.

The scope of this disclosure is to be broadly construed. The embodimentsherein can be used together, separately, mixed or combined. It isintended that this disclosure disclose equivalents, means, systems andmethods to achieve the devices, designs, operations, control systems,controls, activities, mechanical actions, dynamics and results disclosedherein. For each compound, process, method, manufacturing method,mechanical element or mechanism disclosed, it is intended that thisdisclosure also encompasses within the scope of its disclosure andteaches equivalents, means, systems and methods for practicing the manyaspects, compounds, processes, mechanisms and devices disclosed herein.The claims of this application are likewise to be broadly construed.

The description of the technology herein in its many and variedembodiments is merely exemplary in nature and, thus, variations that donot depart from the gist of the disclosure are intended to be within thescope of the claims and the disclosure herein. Such variations are notto be regarded as a departure from the spirit and scope of the disclosedtechnologies.

It will be appreciated that various modifications and changes can bemade to the above-described embodiments of the processes and resultingchemical products as disclosed herein without departing from the spiritand the scope of the claims.

1. A process, comprising the steps of: providing CO and H2; providing afirst catalyst which is an organometallic complex of rhodium and onetype of an organophosphorus ligand or an organometallic complex ofrhodium and more than one type of an organophosphorus ligand; providinga linear alpha olefin; isomerizing said linear alpha olefin by saidfirst catalyst in the presence of CO and H2 at a first pressure toproduce an isomerized olefin; and hydroformylating said isomerizedolefin by said first catalyst in the presence of CO and H2 at a secondpressure different from said first pressure to produce a branchedaldehyde.
 2. The process according to claim 1, wherein said branchedaldehyde is a 2-alkyl branched aldehyde.
 3. The process according toclaim 1, wherein said linear alpha olefin is a C4-C36 linear alphaolefin.
 4. The process according to claim 1, wherein said branchedaldehyde produced from a C4-C36 linear alpha olefin comprises a C5-C37branched aldehyde.
 5. The process according to claim 1, wherein saidlinear alpha olefin is a 1-Butene and said branched aldehyde comprises abranched Pentanal.
 6. The process according to claim 1, wherein saidlinear alpha olefin is a 1-Hexene and said branched aldehyde comprises abranched Heptanal.
 7. The process according to claim 1, wherein saidlinear alpha olefin is a 1-Octene and said branched aldehyde comprises abranched Nonanal.
 8. The process according to claim 1, wherein saidlinear alpha olefin is a 1-Decene and said branched aldehyde comprises abranched Undecanal.
 9. The process according to claim 1, wherein saidlinear alpha olefin is a 1-Dodecene and said branched aldehyde comprisesa branched Tridecanal.
 10. The process according to claim 1, whereinsaid linear alpha olefin is a 1-Tetradecene and said branched aldehydecomprises a branched Pentadecanal.
 11. The process according to claim 1,wherein said linear alpha olefin is a 1-Hexadecene and said branchedaldehyde comprises a branched Heptadecanal.
 12. The process according toclaim 1, wherein said linear alpha olefin is a 1-Octadecene and saidbranched aldehyde comprises a branched Nonadecanal.
 13. The processaccording to claim 1, wherein the organophosphorous ligand can be aphosphine.
 14. The process according to claim 1, wherein the phosphineligand can be triphenylphosphine.
 15. The process according to claim 1,wherein the organophosphorous ligand can be a phosphite.
 16. The processaccording to claim 1, wherein the phosphite ligand can be tris(2,4-di-t-butylphenyl)phosphite.
 17. The process according to claim 1,wherein a mixture of organophosphorous ligands of different types can beused, such as a mixture of a phosphine and a phosphite.
 18. The processaccording to claim 1, wherein a mixture of organophosphorous ligands ofdifferent types can be a mixture of triphenylphosphine and tris(2,4-di-t-butylphenyl)phosphite.
 19. The process according to claim 1,wherein said first catalyst is formed when the molar ratio ofphosphorous to rhodium in a range of 1:1 to 1000:1.